Assay Details
Target Gene Details
Entrez Gene ID: | 79137 |
Gene Name: | family with sequence similarity 134 member A |
Gene Aliases: |
C2orf17, MAG-2 |
Location: |
Chr.2:219178190-219185475 on Build GRCh38 |
Assay Gene Location: | Within Exon 9 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FAM134A | NM_001321109.1 | 9 | 1252 | NP_001308038.1 |
| NM_001321110.1 | 8 | 1109 | NP_001308039.1 | |
| NM_024293.5 | 9 | 1340 | NP_077269.3 | |
| XM_005246848.2 | 9 | 1313 | XP_005246905.1 | |
| AK074983.1 | 9 | 1299 | BAC11332.1 | |
| AK091011.1 | 9 | 936 | ||
| AL832843.1 | 3 | 344 | ||
| AL833630.1 | 2 | 260 | ||
| BC064950.1 | 3 | 396 | AAH64950.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv3170 | Chr.2:219173471 - 219201899 on Build GRCh38 | Deletion |
|
| nsv508200 | Chr.2:219134744 - 219202175 on Build GRCh38 | Deletion |
|
| esv3893555 | Chr.2:219172722 - 219273269 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs535739038] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
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Genomic Map